MANAGEMENT OF ENDOCRINE DISEASE: Recurrence or new tumors after complete resection of pheochromocytomas and paragangliomas: a systematic review and meta-analysisReportar como inadecuado




MANAGEMENT OF ENDOCRINE DISEASE: Recurrence or new tumors after complete resection of pheochromocytomas and paragangliomas: a systematic review and meta-analysis - Descarga este documento en PDF. Documentación en PDF para descargar gratis. Disponible también para leer online.

* Corresponding author 1 UPD5 Médecine - Université Paris Descartes - Faculté de Médecine 2 HEGP - Hôpital Européen Georges Pompidou APHP 3 PARCC - Paris-Centre de recherche Cardiovasculaire Hôpital européen Georges-Pompidou 4 Radboud University Medical Center Nijmegen 5 Carl Gustav Carus University Hospital 6 UPMC - Université Pierre et Marie Curie - Paris 6 - UFR de Médecine Pierre et Marie Curie 7 LIMICS - Laboratoire d-Informatique Médicale et Ingénierie des Connaissances en e-Santé 8 Service de Médecine Interne CHU Tenon

Abstract : Objectives To systematically review the incidence and factors associated with recurrences or new tumors after apparent complete resection of pheochromocytoma or thoraco–abdomino–pelvic paraganglioma.Design A systematic review and meta-analysis of published literature was performed.Methods Pubmed and Embase from 1980 to 2012 were searched for studies published in English on patients with non-metastatic pheochromocytoma or thoraco–abdomino–pelvic paraganglioma, complete tumor resection, postoperative follow-up exceeding 1 month, and recurrence or new tumor documented by pathology, hormonal dosages, or imaging tests. Incidence rates of new events after curative surgery were calculated for each study that had sufficient information and pooled using random-effect meta-analysis.Results In total, 38 studies were selected from 3518 references, of which 36 reported retrospective cohorts from the USA, Europe, and Asia. Patient follow-up was neither standardized nor exhaustive in the included studies. A clear description of patient retrieval methods was available for nine studies and the follow-up protocol and patient flow for four studies. Only two studies used multivariable methods to assess potential predictors of postoperative events.The overall rate of recurrent disease from 34 studies was 0.98 events-100 person-years 95% confidence interval 0.71, 1.25. Syndromic diseases and paragangliomas were consistently associated with a higher risk of a new event in individual studies and in meta-regression analysis.Conclusions The risk of recurrent disease after complete resection of pheochromocytoma may be lower than that previously estimated, corresponding to five events for 100 patients followed up for 5 years after complete resection. Risk stratification is required to tailor the follow-up protocol after complete resection of a pheochromocytoma or paraganglioma. Large multicenter studies are needed to this end.

Keywords : Follow-up Recurrence Risk Factors Paraganglioma Phaeochromocytoma





Autor: Laurence Amar - Charlotte Lussey-Lepoutre - Jacques W M Lenders - Juliette Djadi-Prat - Pierre-Francois Plouin - Olivier Steichen

Fuente: https://hal.archives-ouvertes.fr/



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